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nsv6685232

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:32,333

    Links to Other Resources

    Source: NCBI

    Genome View

    Select assembly:
    Overlapping variant regions from other studies: 174 SVs from 27 studies. See in: genome view    
    Submitted genomic143,565,292-143,597,624Question Mark
    Overlapping variant regions from other studies: 174 SVs from 27 studies. See in: genome view    
    Remapped(Score: Perfect):144,322,861-144,355,193Question Mark

    Variant Region Placement Information

    Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
    nsv6685232Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000002.12Chr2143,565,292143,597,624
    nsv6685232RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000002.11Chr2144,322,861144,355,193

    Variant Call Information

    Variant Call IDTypeMethodAnalysis
    nssv18443675deletionSequencingSplit read and paired-end mapping

    Variant Call Placement Information

    Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
    nssv18443675Submitted genomicNC_000002.12:g.143
    565292_143597624de
    l
    GRCh38 (hg38)NC_000002.12Chr2143,565,292143,597,624
    nssv18443675RemappedPerfectNC_000002.11:g.144
    322861_144355193de
    l
    GRCh37.p13First PassNC_000002.11Chr2144,322,861144,355,193

    No validation data were submitted for this variant

    No clinical assertion data were submitted for this variant

    Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

    Genotype Information

    Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
    nssv184436754e-061276196
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